A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17047176



Internal ID99293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:74846410..74846713hg38UCSC Ensembl
chr11:74557455..74557758hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38304
hg19304
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5509132
Supporting Variants
Samples
Known GenesXRRA1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17047176
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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